Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Shahnaz Alamdari"'
Autor:
Alireza Karimi Yazdi, Parvin Akbariasbagh, Yahya Aghighi, Seyyed Reza Raeeskarami, Khadije Toomaj, Sahar Heidari, Shahnaz Alamdari, Leyla Sahebi
Publikováno v:
Journal of Family and Reproductive Health, Vol 15, Iss 4 (2021)
Objective: Kawasaki disease (KD) occurs in five-year-old or younger children. This study aimed to evaluate the impact of high-dose intravenous immunoglobulin plus acetylsalicylic acid therapy on the prevention and treatment of coronary artery lesions
Externí odkaz:
https://doaj.org/article/5d3a106101854b519167a443d1135c0d
Publikováno v:
Journal of Rehabilitation Sciences and Research, Vol 05, Iss 03, Pp 63-67 (2018)
Background: Chronic otitis media with effusion (CME) primarily affects children. Temporary auditory deprivation is a serious complication of this disease and can result in auditory processing disorder, as demonstrated in past studies. The objectiv
Externí odkaz:
https://doaj.org/article/363c3536c4144351a6cc6efda5addf84
Autor:
Shahnaz Alamdari, Alireza Karimi Yazdi, Khadije Toomaj, Yahya Aghighi, Leyla Sahebi, Parvin Akbariasbagh, Seyyed Reza Raeeskarami, Sahar Heidari
Publikováno v:
Journal of Family and Reproductive Health, Vol 15, Iss 4 (2021)
Objective: Kawasaki disease (KD) occurs in five-year-old or younger children. This study aimed to evaluate the impact of high-dose intravenous immunoglobulin plus acetylsalicylic acid therapy on the prevention and treatment of coronary artery lesions
Autor:
Khadije Toomaj, Parvin Akbariasbagh, Alireza Karimi Yazdi, Yahya Aghighi, Seyyed Reza Raeeskarami, Fariba Eslambol Nassaj, Shahnaz Alamdari
Publikováno v:
Auditory and Vestibular Research, Vol 25, Iss 2 (2016)
Background and Aim: Kawasaki disease (KD) is an acute childhood febrile illness with worldwide incidence and the highest incidence occurs in Asian children, with coronary arteritis being the main complication. Sensorineural hearing loss (SNHL) has
Publikováno v:
Audiology, Vol 17, Iss 2, Pp 61-65 (2009)
Background: Fanconi anemia (FA) is an autosomal recessive genetic disorder wich characterized by progressive pancytopenia, multiple congenital anomalies, increased susceptibility to acute myelogenous leukemia and epithelial cancers specially in head